Hyperlysinemia
From Wikipedia, the free encyclopedia
Hyperlysinemia is a hereditary condition characterized by an abnormal increase of lysine in the blood and appears to be benign.
For a thorough scientific overview of errors of lysine metabolism, one can consult chapter 86 of OMMBID[1]. For more online resources and references, see inborn errors of metabolism.
[edit] See also
- Lysinuria
- Saccharopinuria
[edit] References
- ^ Charles Scriver, Beaudet, A.L., Valle, D., Sly, W.S., Vogelstein, B., Childs, B., Kinzler, K.W. (Accessed 2007). The Online Metabolic and Molecular Bases of Inherited Disease. New York: McGraw-Hill. - Summaries of 255 chapters, full text through many universities. There is also the OMMBID blog.